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rs864622374

From SNPedia

Orientationminus
Make rs864622374(-;-)
Make rs864622374(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position95478073
GenePTCH1
is asnp
is mentioned by
dbSNPrs864622374
ebirs864622374
HLIrs864622374
Exacrs864622374
Varsomers864622374
Maprs864622374
PheGenIrs864622374
hapmaprs864622374
1000 genomesrs864622374
hgdprs864622374
ensemblrs864622374
gopubmedrs864622374
geneviewrs864622374
scholarrs864622374
googlers864622374
pharmgkbrs864622374
gwascentralrs864622374
openSNPrs864622374
23andMers864622374
23andMe allrs864622374
SNP Nexus

SNPshotrs864622374
SNPdbers864622374
MSV3drs864622374
GWAS Ctlgrs864622374
Max Magnitude
ClinVar
Risk rs864622374(;)
Alt rs864622374(;)
Reference rs864622374(C;C)
Significance Pathogenic
Disease Gorlin syndrome
Variation info
Gene PTCH1
CLNDBN Gorlin syndrome
Reversed 1
HGVS NC_000009.11:g.98240355delG
CLNSRC
CLNACC RCV000206300.1,